Disease #00300 (PAPA1;PAPB (polydactyly, postaxial, type A1 (PAPA-1, type B included (PAPB))), OMIM:174200)

Official abbreviation PAPA1;PAPB
Name polydactyly, postaxial, type A1 (PAPA-1, type B included (PAPB))
OMIM ID 174200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GLI3
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-01-19 11:19:19 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00095221 - - post axial polydactyly in 4 affected individuals M yes Pakistan Pastoon - - 18y, 12y surgery PAPA1;PAPB - IQCE IQCE 1 4 Muhammad Umair
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